Menkes X linked disease: heterozygous phenotype in uncloned fibroblast cultures.

Author:

Horn N

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference13 articles.

1. A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration;Menkes, J.H.; Alter, M.; Steigleder, G.K.; Weakley, D.R.; Sung, J.H.;Pediatrics,1962

2. Menkes kinky hair syndrome. An inherited defect in copper absorption with widespread effects;Danks, D.M.; Campbell, P.E.; Stevens, B.J.; Mayne, V.; Cartwright, E.;Pediatrics,1972

3. Extra-hepatic storage of copper. A male foetus suspected of Menkes disease;Hum Genet,1975

4. Is Menkes syndrome a copper storage disorder?;Horn, N.; Heydorn, K.; Damsgaard, E.; Tygstrup, I.; Vestermark, S.;Clin Genet,1978

5. Menkes syndrome: subcellular distribution of copper by an ultrastructural histochemical technique;Horn, N.; Jensen, O.A.;Ultrastructural Pathology,1980

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3. Menkes Disease;Atlas of Genetic Diagnosis and Counseling;2012

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5. Favorably skewed X-inactivation accounts for neurological sparing in female carriers of Menkes disease;Clinical Genetics;2011-01-06

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